Megestrol Acetate
- Product NDC
- 63739-549
- 11-digit product format
- 637390549
- Labeler code
- 63739
- Product ID
- 63739-549_dd4d186c-d380-44d4-934f-b6905af263ac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Megestrol Acetate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- McKesson Corporation DBA SKY Packaging
- Application
- ANDA075671
- Marketing category
- ANDA
- Marketing start
- 2021-06-01
- Marketing end
- 0000-00-00
- Substance
- MEGESTROL ACETATE
- Active strength
- 40 mg/mL
- Pharmacologic classes
- Progesterone Congeners [CS],Progestin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-549-51 | 63739054951 | 2 TRAY in 1 CASE (63739-549-51) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE | 2 tray | 2001-07-25 | 0000-00-00 | No | No | Current |
| 63739-549-73 | 63739054973 | 40 CUP, UNIT-DOSE in 1 CASE (63739-549-73) > 10 mL in 1 CUP, UNIT-DOSE (63739-549-72) | | 2021-06-01 | 0000-00-00 | No | No | Current |